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A V Polyakov

Showing results (41-50 of 56) with videos related to

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Neoplasma|July 24, 2020
Identification of large deletions in the APC gene in Russian patients with familial adenomatous polyposisA S Tsukanov, V V Zabnenkova, V P Shubin, et al.
Human Mutation|March 29, 2000
Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patientsI V Mersiyanova, S M Ismailov, A V Polyakov, et al.
International Journal of Pediatric Otorhinolaryngology|July 25, 2020
Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian populationT G Markova, N N Alekseeva, O L Mironovich, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko|June 27, 2022
[Successful microsurgical resection of a large brainstem abscess: case report and literature review]R S Dzhindzhikhadze, O N Dreval, V A Lazarev, et al.
Vestnik Otorinolaringologii|January 17, 2017
[The results of cochlear implantation in the patient with hereditary and non-hereditary hearing loss]G A Tavartkiladze, V V Bakhshinyan, T G Markova, et al.
Vestnik Otorinolaringologii|January 17, 2017
[The clinical definition and etiology of Pendred syndrome (a review of the literature and clinical observations)]T G Markova, E N Geptner, M R Lalayants, et al.
BMC Neurology|August 5, 2020
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian familiesG E Rudenskaya, V A Kadnikova, O P Ryzhkova, et al.
Prenatal Diagnosis|May 1, 1993
Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in RussiaV S Baranov, V N Gorbunova, O V Malysheva, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 12, 2006
Identification of all pachytene bivalents in the common shrew using DAPI-staining of synaptonemal complex spreadsN M Belonogova, T V Karamysheva, L S Biltueva, et al.
Vestnik Otorinolaringologii|August 17, 2018
[The analysis of the association of the polymorphic variants of the TPMT, COMT, and ABCC3 genes with the development of hearing disorders induced by the cisplatin treatment]O L Mironovich, E A Bliznetz, E S Garbaruk, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Neoplasma|July 24, 2020
Identification of large deletions in the APC gene in Russian patients with familial adenomatous polyposisA S Tsukanov, V V Zabnenkova, V P Shubin, et al.
Human Mutation|March 29, 2000
Screening for mutations in the peripheral myelin genes PMP22, MPZ and Cx32 (GJB1) in Russian Charcot-Marie-Tooth neuropathy patientsI V Mersiyanova, S M Ismailov, A V Polyakov, et al.
International Journal of Pediatric Otorhinolaryngology|July 25, 2020
Clinical features of hearing loss caused by STRC gene deletions/mutations in Russian populationT G Markova, N N Alekseeva, O L Mironovich, et al.
Zhurnal Voprosy Neirokhirurgii Imeni N. N. Burdenko|June 27, 2022
[Successful microsurgical resection of a large brainstem abscess: case report and literature review]R S Dzhindzhikhadze, O N Dreval, V A Lazarev, et al.
Vestnik Otorinolaringologii|January 17, 2017
[The results of cochlear implantation in the patient with hereditary and non-hereditary hearing loss]G A Tavartkiladze, V V Bakhshinyan, T G Markova, et al.
Vestnik Otorinolaringologii|January 17, 2017
[The clinical definition and etiology of Pendred syndrome (a review of the literature and clinical observations)]T G Markova, E N Geptner, M R Lalayants, et al.
BMC Neurology|August 5, 2020
KIF1A-related autosomal dominant spastic paraplegias (SPG30) in Russian familiesG E Rudenskaya, V A Kadnikova, O P Ryzhkova, et al.
Prenatal Diagnosis|May 1, 1993
Dystrophin gene analysis and prenatal diagnosis of Duchenne muscular dystrophy in RussiaV S Baranov, V N Gorbunova, O V Malysheva, et al.
Chromosome Research : an International Journal on the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology|September 12, 2006
Identification of all pachytene bivalents in the common shrew using DAPI-staining of synaptonemal complex spreadsN M Belonogova, T V Karamysheva, L S Biltueva, et al.
Vestnik Otorinolaringologii|August 17, 2018
[The analysis of the association of the polymorphic variants of the TPMT, COMT, and ABCC3 genes with the development of hearing disorders induced by the cisplatin treatment]O L Mironovich, E A Bliznetz, E S Garbaruk, et al.
Pageof 6